A pilot study of the analgesia after laparoscopic inguinal hernia repair

A pilot study of the analgesia after laparoscopic inguinal hernia repair - A pilot study of the analgesia after laparoscopic inguinal hernia repair

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000021842

Enrollment

Registered

2016-04-12

Start date

2016-04-12

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inguinal hernia

Interventions

TAP block Celecoxib(200mg) Celecoxib(200mg)+Diclofenac Sodium sup(50mg)

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: Patients who are personally provided written consent after adequately explained about this study

Exclusion criteria

Exclusion criteria: Patients who judged as inadequacy due to other reasons by the doctor

Design outcomes

Primary

Measure	Time frame
Postoperative pain score	—

Secondary

Measure	Time frame
Complications	—

Countries

Japan

Contacts

Public ContactTakuya Saito

Aichi Medical University Gastroenterological Surgery

tsaito0726@gmail.com0561-62-3311

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026